proline and Congenital Hypocupremia

proline has been researched along with Congenital Hypocupremia in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mori, M; Nishimura, M1

Other Studies

1 other study(ies) available for proline and Congenital Hypocupremia

ArticleYear
A serine-to-proline mutation in the copper-transporting P-type ATPase gene of the macular mouse.
    Mammalian genome : official journal of the International Mammalian Genome Society, 1997, Volume: 8, Issue:6

    Topics: Adenosine Triphosphatases; Animals; Carrier Proteins; Cation Transport Proteins; Copper-Transporting ATPases; Deoxyribonuclease BamHI; Disease Models, Animal; Female; Homozygote; Humans; Male; Menkes Kinky Hair Syndrome; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Point Mutation; Proline; Recombinant Fusion Proteins; Sequence Analysis, DNA; Serine

1997